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Trimethyl borate → (5-Ethoxy-2,4-difluorophenyl)boronic acid

HRID 1438148
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HRID 1438148 반응식
Br[C:2]1[CH:7]=[C:6]([O:8][CH2:9][CH3:10])[C:5]([F:11])=[CH:4][C:3]=1[F:12].[Li]CCCC.[B:18](OC)([O:21]C)[O:19]C>C1COCC1>[CH2:9]([O:8][C:6]1[C:5]([F:11])=[CH:4][C:3]([F:12])=[C:2]([B:18]([OH:21])[OH:19])[CH:7]=1)[CH3:10]
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참가 물질

5

반응물 3

HCID 8470Trimethyl borateHCID 579426611-Bromo-2,4-difluoro-5-ethoxybenzeneHCID 178418339Butyllithium

생성물 1

HCID 53216558(5-Ethoxy-2,4-difluorophenyl)boronic acid수율 70%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To 97D (670 mg, 2.83 mmol) in THF (10 mL) was added n-BuLi (1.6M in hexane, 2.3 mL) at −78° C. After stirring for 15 min, trimethyl borate (0.634 mL) was introduced. The mixture was stirred from −78° C. to rt for 5 h before it was quenched by 1N HCl. It was extracted with ethyl acetate. The organic extract was washed with saturated Na2S2O3, brine and dried over MgSO4. The crude product was purified by column chromatography to give 97E (400 mg, 70% yield) as a solid.

후처리

  1. stirringThe mixture was stirred from −78° C. to rt for 5 h before it
  2. customwas quenched by 1N HCl
  3. extractionIt was extracted with ethyl acetate
  4. extractionThe organic extract
  5. washwas washed with saturated Na2S2O3, brine
  6. dry with materialdried over MgSO4
  7. customThe crude product was purified by column chromatography

출처 및 근거

ORD 기록
ord-ca55ddf56e0d445ca23eb406d987d1f9
출처 데이터셋
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07622585B2

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